510(k) K132008 ยท DTD Pacemaker Lead Adaptor
6981M LEAD EXTENDER KIT, 6984M LEAD EXTENDER KIT, 6986M LEAD EXTENDER KIT, 5866-24M LEAD ADAPTOR KIT, 5866-38M LEAD ADAP
| Applicant | Medtronic, Inc., Mounds View MN, US |
| Decision | Substantially Equivalent, Jul 30, 2013 |
| Received | Jul 1, 2013 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K132008
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.